# positions[].label
Regents Professor and Presidential Impact Fellow

# positions[].organizations[].label
Center for Microencapsulation and Drug Delivery

# positions[].organizations[].parent[].label
Texas A&M University Naresh K. Vashisht College of Medicine

# overview
Dr. Mansoor A. Khan serves as a professor and Vice Dean of the Texas A&M University Rangel College of Pharmacy at College Station, Texas. Prior to joining Texas A&M in 2015, he served as the Director of Product Quality Research and a Senior Biomedical Research Scientist (SBRS) at CDER in US Food and Drug Administration for over eleven years. In FDA, he led the research and review teams to promote manufacturing science, and served as a founding member of the FDA Emerging Technology Team. Dr. Khan received his Ph.D. degree in industrial pharmacy form St. Johns University in NY. He has published over 335 peer-reviewed manuscripts in pharmaceutical formulations and manufacturing sciences, and delivered over 300 presentations world-wide. Dr. Khan's research, currently supported by the NIH and FDA, spans drug delivery and formulations, and he has received over ten million dollars in funding as a principal investigator.

Dr. Khan has held leadership positions at the AAPS including elected chair of formulations design and development (FDD) section. He serves on the editorial board of Pharmaceutical Technology, International Journal of Pharmaceutics, AAPSPharmsciTech, and the Drug Delivery and Translational Research. He has received about 20 FDA/CDER review, research, and exemplary achievement awards, outstanding alumni award at St. Johns University College of Pharmacy, Excellence Award in Texas A&M University. He received the 2012 AAPS Research Achievement Award in Formulations Design and Development. He is also an AAPS and AAiPS Fellow. Dr. Khan served as FDA representative to the World Health Organization (WHO), United States Pharmacopoeia (USP), European Medicine Agency (EMA), DARPA, NIH, National Institute of Pharmaceutical Technology and Education (NIPTE), and International Pharmaceutical Federation (FIP). He is also a member of the European Union Academy of Sciences.

# keywords[]
Principal Component Analysis (pca)-based Process Trajectory

# keywords[]
United States Food And Drug Administration

# keywords[]
Critical Quality Attributes Droplet Size

# keywords[]
United States Food And Drug Administration

# keywords[]
5 Development Of Treatments And Therapeutic Interventions

# keywords[]
3214 Pharmacology And Pharmaceutical Sciences

# keywords[]
5 Development Of Treatments And Therapeutic Interventions

# keywords[]
United States Food And Drug Administration

# keywords[]
United States Food And Drug Administration

# keywords[]
United States Food And Drug Administration

# keywords[]
United States Food And Drug Administration

# keywords[]
United States Food And Drug Administration

# keywords[]
3214 Pharmacology And Pharmaceutical Sciences

# keywords[]
5 Development Of Treatments And Therapeutic Interventions

# keywords[]
3214 Pharmacology And Pharmaceutical Sciences

# keywords[]
United States Food And Drug Administration

# keywords[]
Extended Release, In-use Stability, Dissolution

# keywords[]
United States Food And Drug Administration

# keywords[]
5 Development Of Treatments And Therapeutic Interventions

# keywords[]
9 Industry, Innovation And Infrastructure

# keywords[]
5 Development Of Treatments And Therapeutic Interventions

# keywords[]
United States Food And Drug Administration

# keywords[]
9 Industry, Innovation And Infrastructure

# keywords[]
3214 Pharmacology And Pharmaceutical Sciences

# keywords[]
3214 Pharmacology And Pharmaceutical Sciences

# keywords[]
5 Development Of Treatments And Therapeutic Interventions

# keywords[]
United States Food And Drug Administration

# keywords[]
United States Food And Drug Administration

# keywords[]
United States Food And Drug Administration

# educationAndTraining[].organization.label
Andhra University - (Visakhapatnam, Andhra Pradesh, India)

# educationAndTraining[].organization.label
Idaho State University - (Pocatello, Idaho, United States)

# educationAndTraining[].field
Pharmaceutics (focus on Physical Pharmacy and Drug Delivery System)

# educationAndTraining[].organization.label
St. John's University - (New York, New York, United States)

# educationAndTraining[].field
Pharmaceutics (focus on Industrial Pharmacy and Biopharmaceutics)

# awardsAndHonors[].label
AAPS Excellence in Ligand Binding Assays

# publications[].label
Evaluation of In-Use Stability of Anticoagulant Drug Products: Warfarin Sodium.

# publications[].label
Influence of formulation and processing factors on stability of levothyroxine sodium pentahydrate.

# publications[].label
Use of Hydrogenophaga pseudoflava penetration to quantitatively assess the impact of filtration parameters for 0.2-micrometer-pore-size filters.

# publications[].label
Product and process understanding of a novel pediatric anti-HIV tenofovir niosomes with a high-pressure homogenizer.

# publications[].label
Analytical methods for the evaluation of melamine contamination.

# publications[].label
Quality-by-Design (QbD): Examining the impact of process variables on particle size distribution for a pharmaceutical co-precipitation process using real-time Lasentec FBRM and PVM process monitoring and design of experiments (DOE) approach

# publications[].label
Development and Validation Of A Discriminatory Dissolution Method for Portioned Moist Snuff and Snus.

# publications[].label
Stability characterization of controlled release coprecipitates and solid dispersions.

# publications[].label
Atenolol gastrointestinal therapeutic system: optimization of formulation variables using response surface methodology

# publications[].label
An integrated Quality-by-Design (QbD) approach for pharmaceutical powder blending unit operation: Process monitoring, endpoint determination, and concentration quantification

# publications[].label
Quality by design approach for understanding the critical quality attributes of cyclosporine ophthalmic emulsion.

# publications[].label
Honey, a prospective antibiotic: extraction, formulation, and stability.

# publications[].label
Non-destructive methods of characterization of risperidone solid lipid nanoparticles.

# publications[].label
Comparative evaluation of flow for pharmaceutical powders and granules.

# publications[].label
Scientific and Regulatory Overview of Process Analytical Technology in Bioprocesses

# publications[].label
Real-time monitoring of selective laser sintering 3D printing process for lamivudine content quantification in the printlets: a modern solution to a modern problem.

# publications[].label
Liposome Formation Using a Coaxial Turbulent Jet in Co-Flow.

# publications[].label
Stability characterization and appearance of particulates in a lyophilized formulation of a model peptide hormone-human secretin.

# publications[].label
Defining Patient Centric Pharmaceutical Drug Product Design.

# publications[].label
Focused beam reflectance measurement to monitor nimodipine precipitation process.

# publications[].label
Tablet splitting: Product quality assessment of metoprolol succinate extended release tablets.

# publications[].label
Optimization and characterization of controlled release multi-particulate beads coated with starch acetate.

# publications[].label
Development and Application of a Validated HPLC Method for the Determination of Clindamycin Palmitate Hydrochloride in Marketed Drug Products: An Optimization of the Current USP Methodology for Assay

# publications[].label
Oral delivery of proteins: progress and prognostication.

# publications[].label
Salbutamol sulfate suppositories: influence of formulation on physical parameters and stability.

# publications[].label
Development of Methamphetamine Abuse-Deterrent Formulations Using Sucrose Acetate Isobutyrate.

# publications[].label
Development of a HPLC method for the determination of cyclosporin-A in rat blood and plasma using naproxen as an internal standard.

# publications[].label
Process analytical technology: non-destructive assessment of anastrozole entrapment within PLGA microparticles by near infrared spectroscopy and chemical imaging.

# publications[].label
Response surface methodology for optimization and characterization of limonene-based coenzyme Q10 self-nanoemulsified capsule dosage form.

# publications[].label
Physicochemical and mechanical properties of carbamazepine cocrystals with saccharin.

# publications[].label
Molecular weight determination for colloidal iron by Taguchi optimized validated gel permeation chromatography.

# publications[].label
Considerations for a Pediatric Biopharmaceutics Classification System (BCS): application to five drugs.

# publications[].label
Absorption enhancers in pulmonary protein delivery.

# publications[].label
High Dose Vardenafil Blunts the Hypertensive Effects of Toll-Like Receptor 3 Activation During Pregnancy

# publications[].label
Application of a novel latex on ibuprofen pellets

# publications[].label
A Quality by Design (QbD) approach for pharmaceutical capsule filling unit operation: Identifying critical process variables and detecting possible interactions

# publications[].label
Preparation and in vitro characterization of self-nanoemulsified drug delivery systems of coenzyme Q10 using chiral essential oil components

# publications[].label
Aqueous-Based Cellulose Acetate Butyrate Dispersion: Screening of Process and Formulation Variables to Obtain Verapamil HCl-Controlled Release Beads

# publications[].label
Quantitative evaluation of the thallium binding of soluble and insoluble Prussian blue hexacyanoferrate analogs: A scientific comparison based on their critical quality attributes.

# publications[].label
Tacrolimus properties and formulations: Potential impact of product quality on safety and efficacy

# publications[].label
Regional permeability of coenzyme Q10 in isolated rat gastrointestinal tracts.

# publications[].label
Quality by Design (QbD), Biopharmaceutical Manufacture

# publications[].label
An index for evaluating difficulty of Chewing Index for chewable tablets.

# publications[].label
Chapter 46 Printing of personalized medication using binder jetting 3D printer

# publications[].label
Effect of permeation enhancers on the release of ketoprofen through transdermal drug delivery systems.

# publications[].label
Blend of cellulose ester and enteric polymers for delayed and enteric coating of core tablets of hydrophilic and hydrophobic drugs.

# publications[].label
Bioavailability assessment of oral coenzyme Q10 formulations in dogs.

# publications[].label
Stability Characterization, Kinetics and Mechanism of Degradation of Dantrolene in Aqueous Solution: Effect of pH and Temperature

# publications[].label
Permeability characteristics of novel mydriatic agents using an in vitro cell culture model that utilizes SIRC rabbit corneal cells.

# publications[].label
Real time monitoring of bioreactor mAb IgG3 cell culture process dynamics via Fourier transform infrared spectroscopy: Implications for enabling cell culture process analytical technology

# publications[].label
A validated HPLC assay for simultaneous analysis of salmon calcitonin and duck ovomucoid.

# publications[].label
Statistical Optimization of Ketoprofen-Eudragit S100 Coprecipitates to Obtain Controlled-Release Tablets

# publications[].label
A QbD case study: Bayesian prediction of lyophilization cycle parameters.

# publications[].label
Physico-mechanical and stability evaluation of carbamazepine cocrystal with nicotinamide.

# publications[].label
Formulation and process factors influencing product quality and in vitro performance of ophthalmic ointments.

# publications[].label
Understanding pharmaceutical quality by design.

# publications[].label
Biodegradable microparticulates of beta-estradiol: preparation and in vitro characterization.

# publications[].label
Consistency of Pharmaceutical Products: An FDA Perspective on Hot-Melt Extrusion Process

# publications[].label
In vitro bioequivalence approach for a locally acting gastrointestinal drug: lanthanum carbonate.

# publications[].label
Pyrimethamine 3D printlets for pediatric toxoplasmosis: design, pharmacokinetics, and anti-toxoplasma activity.

# publications[].label
Oral Delivery of Proteins: Effect of Chicken and Duck Ovomucoid on the Stability of Insulin in the Presence of Chymotrypsin and Trypsin

# publications[].label
Response surface methodology for the optimization of ubiquinone self-nanoemulsified drug delivery system.

# publications[].label
Application of salt engineering to reduce/mask bitter taste of clindamycin.

# publications[].label
Quality by design in formulation and process development for a freeze-dried, small molecule parenteral product: a case study.

# publications[].label
Cataplasm-based controlled drug delivery: development and optimization of a novel formulation.

# publications[].label
Preparation and Characterization of 3D-Printed Dose-Flexible Printlets of Tenofovir Disoproxil Fumarate.

# publications[].label
Additive Manufacturing with 3D Printing: Progress from Bench to Bedside.

# publications[].label
Orally disintegrating tablet of novel salt of antiepileptic drug: formulation strategy and evaluation.

# publications[].label
Development of Abuse-Deterrent Formulations Using Sucrose Acetate Isobutyrate.

# publications[].label
Challenges of pediatric formulations: a FDA science perspective.

# publications[].label
Critical Importance and Quality Evaluation of Drug Delivery Autoinjectors in the FDA-DOD Shelf Life Extension Program (SLEP).

# publications[].label
Long-term stability study of Prussian blue-A quality assessment of water content and cyanide release.

# publications[].label
Application of quality by design principles to development of freeze-dried parenteral dosage forms

# publications[].label
Pharmaceutical and Clinical Calculations, 2nd Edition

# publications[].label
Improved Stability of a Model IgG3 by DoE-Based Evaluation of Buffer Formulations.

# publications[].label
Complexation between risperidone and amberlite resin by various methods of preparation and binding study

# publications[].label
A simple HPLC method for the simultaneous analysis of insulin and ovomucoid.

# publications[].label
Response surface methodology to obtain naproxen controlled release tablets from its microspheres with Eudragit L100-55.

# publications[].label
Quality-by-design (QbD): an integrated approach for evaluation of powder blending process kinetics and determination of powder blending end-point.

# publications[].label
Optimization of a self-nanoemulsified tablet dosage form of Ubiquinone using response surface methodology: effect of formulation ingredients.

# publications[].label
Kinetics of drug release from ointments: Role of transient-boundary layer.

# publications[].label
Essential Math and Calculations for Pharmacy Technicians

# publications[].label
An integrated process analytical technology (PAT) approach to monitoring the effect of supercooling on lyophilization product and process parameters of model monoclonal antibody formulations.

# publications[].label
Quality-by-design (QbD): effects of testing parameters and formulation variables on the segregation tendency of pharmaceutical powder measured by the ASTM D 6940-04 segregation tester.

# publications[].label
Quantitative determination of cesium binding to ferric hexacyanoferrate: Prussian blue.

# publications[].label
Optimization and characterization of controlled release pellets coated with an experimental latex: I. Anionic drug

# publications[].label
Captopril gastrointestinal therapeutic system coated with cellulose acetate pseudolatex: evaluation of main effects of several formulation variables.

# publications[].label
Engineering considerations on modeling for pharmaceutical process analytical technology (PAT) applications

# publications[].label
Process QbD case study: An integrated PAT approach for a dynamic pharmaceutical coprecipitation process characterization and process design space development

# publications[].label
Effect of ethanol on opioid drug permeability through caco-2 cell monolayers.

# publications[].label
Development of performance matrix for generic product equivalence of acyclovir topical creams.

# publications[].label
Fermentanomics: Relating quality attributes of a monoclonal antibody to cell culture process variables and raw materials using multivariate data analysis.

# publications[].label
A quantitative study of the effect of process parameters on key granule characteristics in a high shear wet granulation process involving a two component pharmaceutical blend

# publications[].label
Quality-by-design as applied to the development and manufacturing of a lyophilized protein product

# publications[].label
A report from the pediatric formulations task force: perspectives on the state of child-friendly oral dosage forms.

# publications[].label
Implementation of a New Course with a Focus on Active Learning Through Integrated Curricular Approach: Pharmacy Care Laboratory I

# publications[].label
Process QbD case study: An integrated PAT approach for a dynamic pharmaceutical coprecipitation process characterization and process design space development

# publications[].label
Box-behnken design for the optimization of formulation variables of indomethacin coprecipitates with polymer mixtures

# publications[].label
Effect of menthol on permeability of an optically active and racemic propranolol across guinea pig skin.

# publications[].label
Preparation and in vitro characterization of self-nanoemulsified drug delivery system (SNEDDS) of all-trans-retinol acetate.

# publications[].label
Regulatory Perspective on the Development of Polymer Nanomaterials

# publications[].label
Scientific validation of THz spectroscopic measurement and its pharmaceutical process analytical technology (PAT) applications: Case studies of first principles modeling approach

# publications[].label
A quality by design (QbD) case study on liposomes containing hydrophilic API: I. Formulation, processing design and risk assessment.

# publications[].label
A simplified chromatographic method for quantitative determination of coenzyme Q10 in dog plasma.

# publications[].label
Spectroscopic-Based Chemometric Models for Quantifying Low Levels of Solid-State Transitions in Extended Release Theophylline Formulations.

# publications[].label
Quantitative estimation of phenytoin sodium disproportionation in the formulations using vibration spectroscopies and multivariate methodologies.

# publications[].label
Development and validation of X-ray diffraction method for quantitative determination of crystallinity in warfarin sodium products.

# publications[].label
In-Situ Implant Formulation of Laurate and Myristate Prodrugs of Dolutegravir for Ultra-Long Delivery.

# publications[].label
In-use stability assessment of FDA approved metformin immediate release and extended release products for N-Nitrosodimethylamine and dissolution quality attributes.

# publications[].label
Controlled release of a self-emulsifying formulation from a tablet dosage form: stability assessment and optimization of some processing parameters.

# publications[].label
Understanding the effects of formulation and process variables on the printlets quality manufactured by selective laser sintering 3D printing.

# publications[].label
Evaluation of transmission and reflection modalities for measuring content uniformity of pharmaceutical tablets with near-infrared spectroscopy.

# publications[].label
In Vitro and In Vivo Characterization of the Transdermal Gel Formulation of Desloratadine for Prevention of Obesity and Metabolic Syndrome.

# publications[].label
Use of in vitro-in vivo correlation to predict the pharmacokinetics of several products containing a BCS class 1 drug in extended release matrices.

# publications[].label
Opportunities and Challenges of Selective Laser Sintering 3D Printing in Personalized Pharmaceutical Manufacturing

# publications[].label
Risk based in vitro performance assessment of extended release abuse deterrent formulations.

# publications[].label
Online monitoring of PLGA microparticles formation using Lasentec focused beam reflectance (FBRM) and particle video microscope (PVM).

# publications[].label
Process analytical technology: nondestructive evaluation of cyclosporine A and phospholipid solid dispersions by near infrared spectroscopy and imaging.

# publications[].label
Application of quality by design elements for the development and optimization of an analytical method for protamine sulfate.

# publications[].label
Drug product characterization by macropixel analysis of chemical images.

# publications[].label
Chemometric methods for the quantification of crystalline tacrolimus in solid dispersion by powder X-ray diffractrometry.

# publications[].label
The Science and Regulatory Perspectives of Pharmaceutical Suspensions

# publications[].label
Development and application of a validated HPLC method for the analysis of dissolution samples of levothyroxine sodium drug products.

# publications[].label
The evolution of FDA's role in ensuring product quality

# publications[].label
Dose Uniformity of Scored and Unscored Tablets: Application of the FDA Tablet Scoring Guidance for Industry

# publications[].label
Optimization and characterization of controlled release pellets coated with an experimental latex: II. Cationic drug

# publications[].label
Product and process understanding to relate the effect of freezing method on glycation and aggregation of lyophilized monoclonal antibody formulations.

# publications[].label
Permeability of a soft steroid, loteprednol etabonate, through an excised rabbit cornea.

# publications[].label
Cytotoxicity evaluation of enzyme inhibitors and absorption enhancers in Caco-2 cells for oral delivery of salmon calcitonin.

# publications[].label
Regional permeability of salmon calcitonin in isolated rat gastrointestinal tracts: Transport mechanism using Caco-2 cell monolayer

# publications[].label
Crystallinity evaluation of tacrolimus solid dispersions by chemometric analysis.

# publications[].label
An integrated Process Analytical Technology (PAT) approach to examine the effect of temperature on nucleation kinetics of a dynamic pharmaceutical co-precipitation process

# publications[].label
Application of chemometric methods to differential scanning calorimeter (DSC) to estimate nimodipine polymorphs from cosolvent system.

# publications[].label
PROCESS CONTROL PERSPECTIVE FOR PROCESS ANALYTICAL TECHNOLOGY: INTEGRATION OF CHEMICAL ENGINEERING PRACTICE INTO SEMICONDUCTOR AND PHARMACEUTICAL INDUSTRIES

# publications[].tags
9 Industry, Innovation and Infrastructure

# publications[].label
Development of a Validated Stability Indicating HPLC Method for Ranitidine Hydrochloride Syrup

# publications[].label
Oral delivery of salmon calcitonin with ovomudoids

# publications[].label
Pharmaceutical characterization of novel tenofovir liposomal formulations for enhanced oral drug delivery: in vitro pharmaceutics and Caco-2 permeability investigations.

# publications[].label
Controlled release multiparticulate beads coated with starch acetate: material characterization, and identification of critical formulation and process variables.

# publications[].label
Hunter screening design to understand the product variability of solid dispersion formulation of a peptide antibiotic.

# publications[].label
Stability of ranitidine syrup re-packaged in unit-dose containers.

# publications[].label
Influence of tablet characteristics on weight variability and weight loss in split tablets.

# publications[].label
Physicochemical characterization of complex drug substances: evaluation of structural similarities and differences of protamine sulfate from various sources.

# publications[].label
Formulation and evaluation of a protein-loaded solid dispersions by non-destructive methods.

# publications[].label
Effects of excipients and curing process on the abuse deterrent properties of directly compressed tablets.

# publications[].label
Use of SIRC Rabbit Corneal Cell Lines Grown on Polycarbonate- or Polyester-Based Filters to Assess the In Vitro Corneal Transport/Toxicity Screening Using Pilocarpine With or Without Benzalkonium Chloride

# publications[].label
Comparative evaluation of controlled-release solid oral dosage forms prepared with solid dispersions and coprecipitates

# publications[].label
Preparation and characterization of a suite of ephedra-containing standard reference materials.

# publications[].label
Analysis of ubidecarenone (CoQ10) aqueous samples using reversed phase liquid chromatography.

# publications[].label
Challenges, opportunities, and scientific aspects of implementing pat in biopharmaceuticals

# publications[].label
Racemate and enantiomers of ketoprofen: phase diagram, thermodynamic studies, skin permeability, and use of chiral permeation enhancers.

# publications[].label
Comparison of Univariate and Multivariate Models of C SSNMR and XRPD Techniques for Quantification of Nimodipine Polymorphs.

# publications[].label
Real-time on-line blend uniformity monitoring using near-infrared reflectance spectrometry: a noninvasive off-line calibration approach.

# publications[].label
3D-printing of lopinavir printlets by selective laser sintering and quantification of crystalline fraction by XRPD-chemometric models.

# publications[].label
Disintegration of highly soluble immediate release tablets: a surrogate for dissolution.

# publications[].label
Polymethacrylate based microparticulates of insulin for oral delivery, part II: solid state characterization.

# publications[].label
Regulatory Issues and Challenges Associated with the Development of Performance Specifications for Modified Release Parenteral Products

# publications[].tags
9 Industry, Innovation and Infrastructure

# publications[].label
Development and application of a validated HPLC method for the determination of gabapentin and its major degradation impurity in drug products.

# publications[].label
Aqueous-based polymeric dispersion: preparation and characterization of cellulose acetate pseudolatex

# publications[].label
HIV-1 Tat and cocaine impact astrocytic energy reservoir influence on miRNA epigenetic regulation.

# publications[].label
A Dual Controlled Gastrointestinal Therapeutic System of Salmon Calcitonin. II. Screening of Process and Formulation Variables

# publications[].label
Naproxen-Eudragit microspheres: screening of process and formulation variables for the preparation of extended release tablets.

# publications[].label
Chemometric evaluation of near infrared, fourier transform infrared, and Raman spectroscopic models for the prediction of nimodipine polymorphs.

# publications[].label
Regulatory Aspects of Nanomaterial Applications in Pharmaceutical Industry

# publications[].label
Artificial neural network and simplex optimization for mixing of aqueous-coated beads to obtain controlled-release formulations

# publications[].label
Chain length-dependent effects of alkylmaltosides on nasal absorption of enoxaparin.

# publications[].label
An Integrated Process Analytical Technology (PAT) Approach for Process Dynamics-Related Measurement Error Evaluation and Process Design Space Development of a Pharmaceutical Powder Blending Bed

# publications[].label
Development and Validation of a Discriminatory Dissolution Method for Rifaximin Products.

# publications[].label
Selective laser sintering 3D printing - an overview of the technology and pharmaceutical applications.

# publications[].label
Stability of gabapentin 300-mg capsules repackaged in unit dose containers.

# publications[].label
A small variation in average particle size of PLGA nanoparticles prepared by nanoprecipitation leads to considerable change in nanoparticles' characteristics and efficacy of intracellular delivery.

# publications[].label
Compression of Indomethacin Coprecipitates with Polymer Mixtures: Effect of Preparation Methodology

# publications[].label
Nanoparticle technology for drug delivery across the blood-brain barrier.

# publications[].label
Evaluation of the In Vitro Efficacy of Sevelamer Hydrochloride and Sevelamer Carbonate.

# publications[].label
HIV-1 Tat and cocaine impact astrocytic energy reservoirs and epigenetic regulation by influencing the LINC01133-hsa-miR-4726-5p-NDUFA9 axis.

# publications[].label
Salt Engineering of Aripiprazole with Polycarboxylic Acids to Improve Physicochemical Properties.

# publications[].label
Comparison of X-ray powder diffraction and solid-state nuclear magnetic resonance in estimating crystalline fraction of tacrolimus in sustained-release amorphous solid dispersion and development of discriminating dissolution method.

# publications[].label
Challenges and Opportunities for Biotech Quality by Design

# publications[].label
Quality-by-design (QbD): an integrated multivariate approach for the component quantification in powder blends.

# publications[].label
Transport studies of insulin across rat jejunum in the presence of chicken and duck ovomucoids.

# publications[].label
Spectral and spatial characterization of protein loaded PLGA nanoparticles.

# publications[].label
Corrigendum: 2007 highlights of advances in the pharmaceutical sciences: An American Association of Pharmaceutical Scientists (AAPS) perspective

# publications[].label
2007 highlights of advances in the pharmaceutical sciences: An American Association of Pharmaceutical Scientists (AAPS) perspective

# publications[].label
Comparison of the stability of split and intact gabapentin tablets.

# publications[].label
Optimization and characterization of controlled release multi-particulate beads formulated with a customized cellulose acetate butyrate dispersion.

# publications[].label
A two-stage reverse dialysis in vitro dissolution testing method for passive targeted liposomes.

# publications[].label
Supramolecular copper hydroxide tennis balls: self-assembly, structures, and magnetic properties of octanuclear [Cu(8)L(8)(OH)(4)](4+) clusters (HL = N-(2-pyridylmethyl)acetamide).

# publications[].label
Stability indicating validated HPLC method for quantification of levothyroxine with eight degradation peaks in the presence of excipients.

# publications[].label
Assessing the impact of nimodipine devitrification in the ternary cosolvent system through quality by design approach.

# publications[].label
Osmotically-controlled oral dosage form of a dipeptide: Screening of formulation variables

# publications[].label
Mapping the state of a pharmaceutical Co-precipitation process: An integrated process analytical technology (PAT) approach

# publications[].label
An Integrated Process Analytical Technology (PAT) Approach for Pharmaceutical Crystallization Process Understanding to Ensure Product Quality and Safety: FDA Scientists Perspective

# publications[].label
Preparation and characterization of genistein containing poly(ethylene glycol) microparticles

# publications[].label
Tablet splitting of a narrow therapeutic index drug: a case with levothyroxine sodium.

# publications[].label
Integration of Near-Infrared Spectroscopy and Mechanistic Modeling for Predicting Film-Coating and Dissolution of Modified Release Tablets

# publications[].label
Formulation Characterization and Pharmacokinetic Evaluation of Amorphous Solid Dispersions of Dasatinib.

# publications[].label
Stereomicroscopic imaging technique for the quantification of cold flow in drug-in-adhesive type of transdermal drug delivery systems.

# publications[].label
FDA: contribution to developing pediatric formulations and transatlantic collaboration.

# publications[].label
Plackett-Burman screening of micromatrices with polymer mixtures for controlled drug delivery

# publications[].label
Intraocular pressure-lowering activity and in vivo disposition of dipivalyl terbutalone in rabbits.

# publications[].label
Development and validation of an ion chromatography method for the determination of phosphate-binding of lanthanum carbonate.

# publications[].label
Quality-by-design (QbD): Process trajectory development for a pharmaceutical co-precipitation process based on an integrated real-time process monitoring strategy

# publications[].label
Preparation and characterization of coenzyme Q10-Eudragit solid dispersion.

# publications[].label
Preparation and Characterization of Stable Amorphous Glassy Solution of BCS II and IV Drugs.

# publications[].label
Impact of formulation and process variables on solid-state stability of theophylline in controlled release formulations.

# publications[].label
Formulation and transport properties of tenofovir loaded liposomes through Caco-2 cell model.

# publications[].label
Improvement of physicochemical properties of an antiepileptic drug by salt engineering.

# publications[].label
Quality-by-design: an integrated process analytical technology approach to determine the nucleation and growth mechanisms during a dynamic pharmaceutical coprecipitation process.

# publications[].label
A quality by design (QbD) case study on liposomes containing hydrophilic API: II. Screening of critical variables, and establishment of design space at laboratory scale.

# publications[].label
Chemometric Models for Quantification of Carbamazepine Anhydrous and Dihydrate Forms in the Formulation.

# publications[].label
Nitroso Impurities in Drug Products: An Overview of Risk Assessment, Regulatory Milieu, and Control Strategy.

# publications[].label
Coating characterization by hyperspectroscopy and predictive dissolution models of tablets coated with blends of cellulose acetate and cellulose acetate phthalate.

# publications[].label
Effect of chiral enhancers on the permeability of optically active and racemic metoprolol across hairless mouse skin.

# publications[].label
Complexation between risperidone and amberlite resin by various methods of preparation and binding study.

# publications[].label
Application of NIR chemometric methods for quantification of the crystalline fraction of warfarin sodium in drug product.

# publications[].label
Difference in the lubrication efficiency of bovine and vegetable-derived magnesium stearate during tabletting.

# publications[].label
Chirality and its implications in transdermal drug development.

# publications[].label
Workshop Report: USP Workshop on Exploring the Science of Drug Absorption

# publications[].label
A headspace-gas chromatography method for isopropanol determination in warfarin sodium products as a measure of drug crystallinity.

# publications[].label
Determination of tacrolimus crystalline fraction in the commercial immediate release amorphous solid dispersion products by a standardized X-ray powder diffraction method with chemometrics.

# publications[].label
Aqueous-based polymeric dispersion: face-centered cubic design for the development of atenolol gastrointestinal therapeutic system.

# publications[].label
United States Food and Drug Administration and Department of Defense shelf-life extension program of pharmaceutical products: progress and promise.

# publications[].label
Formulation Optimization of Selective Laser Sintering 3D-Printed Tablets of Clindamycin Palmitate Hydrochloride by Response Surface Methodology.

# publications[].label
Effectiveness of premedication at the time of separation from parent and mask induction in paediatric patients coming for congenital heart disease surgery.

# publications[].label
Quality by design: characterization of self-nano-emulsified drug delivery systems (SNEDDs) using ultrasonic resonator technology.

# publications[].label
Effect of extragranular microcrystalline cellulose: On compaction, surface roughness, and in vitro dissolution of a self-nanoemulsified solid dosage form of ubiquinone

# publications[].label
A new chapter in pharmaceutical manufacturing: 3D-printed drug products.

# publications[].tags
9 Industry, Innovation and Infrastructure

# publications[].label
Quality and In-Use Stability Comparison of Brand and Generics of Extended-Release Phenytoin Sodium Capsules.

# publications[].label
Assessment of Recent Process Analytical Technology (PAT) Trends: A Multiauthor Review

# publications[].label
Development of a Multivariate Predictive Dissolution Model for Tablets Coated with Cellulose Ester Blends.

# publications[].label
Building better drugs: developing and regulating engineered therapeutic proteins.

# publications[].label
Complexation of risperidone with a taste-masking resin: novel application of near infra-red and chemical imaging to evaluate complexes.

# publications[].label
Permeability of chemical delivery systems across rabbit corneal (SIRC) cell line and isolated corneas: a comparative study.

# publications[].label
Root cause evaluation of particulates in the lyophilized indomethacin sodium trihydrate plug for parenteral administration.

# publications[].label
Potential Application of USP Paddle and Basket Dissolution Methods in Discriminating for Portioned Moist Snuff and Snus Smokeless Tobacco Products.

# publications[].label
Quality-by-Design (QbD): an integrated process analytical technology (PAT) approach for real-time monitoring and mapping the state of a pharmaceutical coprecipitation process.

# publications[].label
Process analytical technology: chemometric analysis of Raman and near infra-red spectroscopic data for predicting physical properties of extended release matrix tablets.

# publications[].label
Thermodynamic stability assessment of a colloidal iron drug product: sodium ferric gluconate.

# publications[].label
Chemometric Model Development and Comparison of Raman and (13)C Solid-State Nuclear Magnetic Resonance-Chemometric Methods for Quantification of Crystalline/Amorphous Warfarin Sodium Fraction in the Formulations.

# publications[].label
Quality by design: impact of formulation variables and their interactions on quality attributes of a lyophilized monoclonal antibody.

# publications[].label
Characterization and in vivo ulcerogenicity study of oral extended release preparations

# publications[].label
Functionality of magnesium stearate derived from bovine and vegetable sources: dry granulated tablets.

# publications[].label
Evaluation of cytotoxicity of oils used in coenzyme Q10 Self-emulsifying Drug Delivery Systems (SEDDS).

# publications[].label
Development and Validation of Matrix of Chemistry, Manufacturing, and Control (MoCMC) System for Intramammary Drug Products (IMM).

# publications[].label
Atenolol Gastrointestinal Therapeutic System. I. Screening of Formulation Variables

# publications[].label
Formulation of anastrozole microparticles as biodegradable anticancer drug carriers.

# publications[].label
Quality by design: understanding the product variability of a self-nanoemulsified drug delivery system of cyclosporine A.

# publications[].label
To investigate the influence of machine operating variables on formulations derived from lactose types in capsule filling: part 2.

# publications[].label
Chemometric Assisted X-Ray Powder Diffractometry Method for Crystalline Lopinavir Quantification in 3D Printlets Manufactured by Selective Laser Sintering

# publications[].label
Effect of temperature and humidity on long term storage of atenolol gastro-intestinal therapeutic system

# publications[].label
HotMelt Extrusion: An FDA Perspective on Product and Process Understanding

# publications[].label
Comparative stability study of unit-dose repackaged furosemide tablets

# publications[].label
THz spectroscopy: An emerging technology for pharmaceutical development and pharmaceutical Process Analytical Technology (PAT) applications

# publications[].label
Fractionated charge variants of biosimilars: A review of separation methods, structural and functional analysis.

# publications[].label
Preparation and characterization of a customized cellulose acetate butyrate dispersion for controlled drug delivery.

# publications[].label
Quality-by-Design (QbD): An integrated process analytical technology (PAT) approach for a dynamic pharmaceutical co-precipitation process characterization and process design space development.

# publications[].label
Effect of menthol and related terpenes on the percutaneous absorption of propranolol across excised hairless mouse skin.

# publications[].label
Influence of drug loading and type of ointment base on the in vitro performance of acyclovir ophthalmic ointment.

# publications[].label
Challenges, opportunities, and scientific aspects of implementing PAT in biopharmaceuticals

# publications[].label
Strategies of targeting oral drug delivery systems to the colon and their potential use for the treatment of colorectal cancer.

# publications[].label
Evaluation of butyrate-induced production of a mannose-6-phosphorylated therapeutic enzyme using parallel bioreactors.

# publications[].label
Optimization and in vivo evaluation of an oral dual controlled-release tablet dosage form of insulin and duck ovomucoid.

# publications[].label
Response surface methodology for the development of self-nanoemulsified drug delivery system (SNEDDS) of all-trans-retinol acetate.

# publications[].label
Chemical delivery systems: evaluation of physicochemical properties and enzymatic stability of phenylephrone derivatives.

# publications[].label
Dose Uniformity of Scored and Unscored Tablets: Application of the FDA Tablet Scoring Guidance for Industry.

# publications[].label
Long-term stability characterization of a controlled release gastrointestinal therapeutic system coated with a cellulose acetate pseudolatex.

# publications[].label
Response surface methodology to obtain beta-estradiol biodegradable microspheres for long-term therapy of osteoporosis.

# publications[].label
In Vitro Drug Transfer Due to Drug Retention in Human Epidermis Pretreated with Application of Marketed Estradiol Transdermal Systems.

# publications[].label
Evaluation of Abuse-Deterrent Characteristics of Tablets Prepared via Hot-Melt Extrusion.

# publications[].label
Comparative stability of repackaged metoprolol tartrate tablets.

# publications[].label
Patient In-Use Stability Testing of FDA-Approved Metformin Combination Products for N-Nitrosamine Impurity.

# publications[].label
Predicting hydrophilic drug encapsulation inside unilamellar liposomes.

# publications[].label
The Science and Regulatory Perspectives of Emerging Controlled Release Dosage Forms

# publications[].label
Binder Jetting Powder Bed 3D Printing for the Fabrication of Drug Delivery System

# publications[].label
Near-infrared investigations of novel anti-HIV tenofovir liposomes.

# publications[].label
Studying effect of glyceryl palmitostearate amount, manufacturing method and stability on polymorphic transformation and dissolution of rifaximin tablets.

# publications[].label
An Enteric DualControlled Gastrointestinal Therapeutic System of Salmon CalcitoninI: Preparation, Characterization, and Preclinical Bioavailability in Rats

# publications[].label
Quality by design: understanding the formulation variables of a cyclosporine A self-nanoemulsified drug delivery systems by Box-Behnken design and desirability function.

# publications[].label
Development and application of a validated stability-indicating Ultra-Performance Liquid Chromatography (UPLC) method for the determination of dantrolene and its related impurities

# publications[].label
Physical characterization and dissolution properties of ibuprofen: Eudragit coprecipitates.

# publications[].label
Participation of women in clinical trials for new drugs approved by the food and drug administration in 2000-2002.

# publications[].label
Targeting to macrophages: role of physicochemical properties of particulate carriers--liposomes and microspheres--on the phagocytosis by macrophages.

# publications[].label
Ibuprofen Release from Beads Coated with an Experimental Latex: Effect of Certain Variables

# publications[].label
Development and validation of in vitro-in vivo correlation (IVIVC) for estradiol transdermal drug delivery systems.

# publications[].label
A mechanistic population balance model for granulation processes: Effect of process and formulation parameters

# publications[].label
Scientific and Regulatory Considerations in Product Development

# publications[].label
Process analytical technology to understand the disintegration behavior of alendronate sodium tablets.

# publications[].label
Assessing impact of formulation and process variables on in-vitro performance of directly compressed abuse deterrent formulations.

# publications[].label
Influence of psychostimulants and opioids on epigenetic modification of class III histone deacetylase (HDAC)-sirtuins in glial cells.

# publications[].label
Withdrawal of generic budeprion for nonbioequivalence.

# publications[].label
Process analytical technology (PAT): effects of instrumental and compositional variables on terahertz spectral data quality to characterize pharmaceutical materials and tablets.

# publications[].label
Effect of Additives on the Diffusion of Ketoprofen Through Human Skin

# publications[].label
Chapter 16 Nanotechnology-based drug products Science and regulatory considerations

# publications[].label
Comparative evaluation of the severity of gastric ulceration by solid dispersions and coprecipitates of indomethacin.

# publications[].label
Cold flow of estradiol transdermal systems: influence of drug loss on the in vitro flux and drug transfer across human epidermis.

# publications[].label
Impact of controlled ice nucleation on process performance and quality attributes of a lyophilized monoclonal antibody.

# publications[].label
Quantitative determination of thallium binding to ferric hexacyanoferrate: Prussian blue.

# publications[].label
Challenges, opportunities, and scientific aspects of implementing PAT in biopharmaceuticals

# publications[].label
HIV-1 Tat and cocaine coexposure impacts piRNAs to affect astrocyte energy metabolism.

# publications[].label
Effect of processing parameters and controlled environment storage on the disproportionation and dissolution of extended-release capsule of phenytoin sodium.

# publications[].label
An integrated process analytical technology (PAT) approach to examine the effect of temperature on nucleation kinetics of a dynamic pharmaceutical coprecipitation process

# publications[].label
Ultra-long acting prodrug of dolutegravir and delivery system - Physicochemical, pharmacokinetic and formulation characterizations.

# publications[].label
Quality-by-design (QbD) for capsule formulation and process development regulatory science relevance, scientific case studies, and future challenges

# publications[].label
Transbuccal permeation of a nucleoside analog, dideoxycytidine: effects of menthol as a permeation enhancer.

# publications[].label
Design, in vitro stability, and ocular hypotensive activity of t-butalone chemical delivery systems.

# publications[].label
Preparation and characterization of dicarboxylic acids salt of aripiprazole with enhanced physicochemical properties.

# publications[].label
Effects of Diluents on Physical and Chemical Stability of Phenytoin and Phenytoin Sodium.

# publications[].label
Self-emulsifying drug delivery systems (SEDDS) of coenzyme Q10: formulation development and bioavailability assessment.

# publications[].label
Formulation and Route of AdministrationInfluencing Drug Permeability and Absorption

# publications[].label
Percutaneous permeation of enantiomers and racemates of chiral drugs and prediction of their flux ratios using thermal data: a pharmaceutical perspective.

# publications[].label
In Vitro and In Vivo testing of 3D-Printed Amorphous Lopinavir Printlets by SelectiveLaser Sinitering: Improved Bioavailability of a Poorly Soluble Drug.

# publications[].label
Bioreactor process parameter screening utilizing a Plackett-Burman design for a model monoclonal antibody.

# publications[].label
Effect of patients in-use and accelerated stability conditions on quality attributes and pharmacokinetic profile of four FDA approved extended-release anti-epileptic-drug products.

# publications[].label
Comparative evaluation of in vitro efficacy of colesevelam hydrochloride tablets.

# publications[].label
Comparative evaluation of the in vitro efficacy of lanthanum carbonate chewable tablets.

# publications[].label
Robust calibration design in the pharmaceutical quantitative measurements with near-infrared (NIR) spectroscopy: Avoiding the chemometric pitfalls.

# publications[].label
Regulatory Considerations in Development of Amorphous Solid Dispersions

# publications[].label
Application of Sucrose Acetate Isobutyrate in Development of Co-Amorphous Formulations of Tacrolimus for Bioavailability Enhancement.

# publications[].label
Combination of Paclitaxel and R-flurbiprofen loaded PLGA nanoparticles suppresses glioblastoma growth on systemic administration.

# publications[].label
Tannate complexes of antihistaminic drug: sustained release and taste masking approaches.

# publications[].label
Chapter 11 Nanoparticles for improvement in oral bioavailability

# publications[].label
Stability and bioequivalence studies of two marketed formulations of coenzyme Q10 in beagle dogs.

# publications[].label
Optimization of process variables for the preparation of ibuprofen coprecipitates with eudragit S100

# publications[].label
Regional permeability of salmon calcitonin in isolated rat gastrointestinal tracts: transport mechanism using Caco-2 cell monolayer.

# publications[].label
Preparation and in vitro characterization of a semi-solid dispersion of flurbiprofen with Gelucire 44/14 and Labrasol.

# publications[].label
Long-term stability study of Prussian blue - a quality assessment of water content and thallium binding.

# publications[].label
Development and validation of a HPLC method for dissolution and stability assay of liquid-filled cyclosporine capsule drug products.

# publications[].label
Characterization and selection of suitable grades of lactose as functional fillers for capsule filling: part 1.

# publications[].label
Formulation and stability evaluation of ketoprofen sustained-release tablets prepared by fluid bed granulation with Carbopol 971P solution.

# publications[].label
Spontaneous carbonate formation in an amorphous, amine-rich, polymeric drug substance: sevelamer HCl product quality.

# publications[].label
Protection of salmon calcitonin breakdown with serine proteases by various ovomucoid species for oral drug delivery.

# publications[].label
Development of stable amorphous solid dispersion and quantification of crystalline fraction of lopinavir by spectroscopic-chemometric methods.

# publications[].label
Patient in-use, room temperature and accelerated conditions stability evaluation of FDA approved clopidogrel hydrogen sulfate products.

# publications[].label
Cholorpheniramine tannate complexes: physicochemical, chemometric, and taste masking evaluation.

# publications[].label
Application of quality by design to formulation and processing of protein liposomes.

# publications[].label
Development and optimization of taste-masked orally disintegrating tablets (ODTs) of clindamycin hydrochloride.

# publications[].label
Solid-state stability assessment of controlled release tablets containing Carbopol 971P.

# publications[].label
Pharmaceutical characterization and thermodynamic stability assessment of a colloidal iron drug product: iron sucrose.

# publications[].label
Very-Rapidly Dissolving Printlets of Isoniazid Manufactured by SLS 3D Printing: In Vitro and In Vivo Characterization.

# publications[].label
Lyophilization of Biologics: An FDA Perspective

# publications[].label
Development and Characterization of Printlets of Lamivudine for Pediatric Patients Using Selective Laser Sintering

# publications[].label
Process analytical technology (PAT): quantification approaches in terahertz spectroscopy for pharmaceutical application.

# publications[].label
THERMAL INFLUENCE ON PRINTLET QUALITY IN THE SELECTIVE LASER SINTERING OF PHARMACEUTICAL FORMULATIONS

# publications[].label
NIR spectroscopy applications in the development of a compacted multiparticulate system for modified release.

# publications[].label
Preparation and in vitro characterization of a eutectic based semisolid self-nanoemulsified drug delivery system (SNEDDS) of ubiquinone: mechanism and progress of emulsion formation.

# publications[].label
Univariate and Multivariate Models for Determination of Prasugrel Base in the Formulation of Prasugrel Hydrochloride Using XRPD Method.

# publications[].label
Development and evaluation of paclitaxel nanoparticles using a quality-by-design approach.

# publications[].label
A long-term stability study of Prussian blue: A quality assessment of water content and cesium binding.

# publications[].label
Formulation Development and Stability Evaluation: Of a Multicomponent Nutritional Supplement

# publications[].label
Calcium Phosphate in Pharmaceutical Product Development

# publications[].label
Synthesis and evaluation of morpholinoalkyl ester prodrugs of indomethacin and naproxen.

# publications[].label
Morpholinoalkyl ester prodrugs of diclofenac: synthesis, in vitro and in vivo evaluation.

# publications[].label
Pharmaceutical coating operations: Challenges and opportunities in the changing regulatory paradigm

# publications[].label
Risperidone solid dispersion for orally disintegrating tablet: its formulation design and non-destructive methods of evaluation.

# publications[].label
Aqueous based polymeric dispersion: Plackett--Burman design for screening of formulation variables of atenolol gastrointestinal therapeutic system.

# publications[].label
Characterization of a nonribosomal peptide antibiotic solid dispersion formulation by process analytical technologies sensors.

# publications[].label
Advancing Product Quality: a Summary of the Inaugural FDA/PQRI Conference.

# publications[].tags
9 Industry, Innovation and Infrastructure

# publications[].label
Process QbD case study: An integrated PAT approach for a dynamic pharmaceutical co-precipitation process characterization and process design space development

# publications[].label
Integrated Process Analytical Technology Approach for Nucleation Induction Time Measurement and Nucleation Mechanism Assessment for a Dynamic Multicomponent Pharmaceutical Antisolvent Crystallization System

# publications[].label
Scientific and Regulatory Considerations in Product Development

# publications[].label
Permeation of genistein through human skin

# publications[].label
Development of curcumin and docetaxel co-loaded actively targeted PLGA nanoparticles to overcome blood brain barrier

# publications[].label
Controlled drug delivery Development of solid oral dosage forms with acrylate polymers

# publications[].label
Quality-by-Design (QbD) case study: Powder blending process kinetics evaluation

# publications[].label
Current status of the oral delivery of insulin

# publications[].label
Near-infrared and fourier transform infrared chemometric methods for the quantification of crystalline tacrolimus from sustained-release amorphous solid dispersion.

# publications[].label
Understanding the quality of protein loaded PLGA nanoparticles variability by Plackett-Burman design.

# publications[].label
FDA Analysis of Atorvastatin Products Refutes Report of Methyl Ester Impurities.

# publications[].label
Polymethyacrylate based microparticulates of insulin for oral delivery: preparation and in vitro dissolution stability in the presence of enzyme inhibitors.

# publications[].label
Data integrity issues in pharmaceutical industry: Common observations, challenges and mitigations strategies.

# publications[].label
Oseltamivir phosphate-amberlite(TM) IRP 64 ionic complex for taste masking: preparation and chemometric evaluation.

# publications[].label
Effect of plasticizer on free volume and permeability in cellulose acetate pseudolatex membranes studied by positron annihilation and tracer diffusion methods

# publications[].label
Polymers in Ophthalmic Drug Delivery Systems

# publications[].label
Scientific validation of THz spectroscopic measurement and its pharmaceutical process analytical technology (PAT) Applications: Case studies of first principles modeling approach

# publications[].label
Monitoring, understanding and assessing pharmaceutical process and product quality

# publications[].label
A Comparative Evaluation of Polystyrene Divinylbenzene Copolymer HPLC Columns on the Chromatographic Performance of the Compendial Method for Doxycycline Hyclate Capsules: Implications for Method Implementation of a Medical Countermeasure Medication

# publications[].label
Development and application of a validated HPLC method for the analysis of dissolution samples of gabapentin drug products.

# publications[].label
Bioavailability assessment of salbutamol sulfate suppositories in human volunteers.

# editorOf[].label
Quality by Design for Biopharmaceutical Drug Product Development

# researcherOn[].label
Dissolution of Smokeless Tobacco Products

# researcherOn[].awardedBy.label
United States Food and Drug Administration - (Silver Spring, Maryland, United States)

# streetAddress
206 Olsen BLVD, Reynolds Medical building; 

# organizations[]
Center for Microencapsulation and Drug Delivery

# organizations[]
Texas A&M University Naresh K. Vashisht College of Medicine

# schools[]
Texas A&M University Naresh K. Vashisht College of Medicine